U.S. patent application number 12/100754 was filed with the patent office on 2008-12-18 for radiation-crosslinking and thermally crosslinking pu systems comprising iminooxadiazinedione.
This patent application is currently assigned to Bayer MaterialScience AG. Invention is credited to Friedrich-Karl Bruder, Frank Richter, Nicolas Stockel.
Application Number | 20080311482 12/100754 |
Document ID | / |
Family ID | 39591625 |
Filed Date | 2008-12-18 |
United States Patent
Application |
20080311482 |
Kind Code |
A1 |
Stockel; Nicolas ; et
al. |
December 18, 2008 |
Radiation-crosslinking and thermally crosslinking PU systems
comprising iminooxadiazinedione
Abstract
The present invention relates to polyurethane compositions which
cure by radiation and thermal action with crosslinking, and use
thereof for the production of holographic media. The polyurethane
compositions of the invention comprise A) one or more
iminooxadiazinedione-group-containing polyisocyanates, B) one or
more polyfunctional, isocyanate-reactive compounds, C) one or more
compounds having groups which on exposure to actinic radiation with
ethylenically unsaturated compounds with polymerization
(radiation-curing groups), D) optionally one or more free radical
stabilizers and E) one or more photoinitiators.
Inventors: |
Stockel; Nicolas; (Koln,
DE) ; Bruder; Friedrich-Karl; (Krefeld, DE) ;
Richter; Frank; (Leverkusen, DE) |
Correspondence
Address: |
Connolly Bove Lodge & Hutz LLP
1007 North Orange Street, P.O. Box 2207
Wilmington
DE
19899-2207
US
|
Assignee: |
Bayer MaterialScience AG
Leverkusen
DE
|
Family ID: |
39591625 |
Appl. No.: |
12/100754 |
Filed: |
April 10, 2008 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
60922989 |
Apr 11, 2007 |
|
|
|
Current U.S.
Class: |
430/2 |
Current CPC
Class: |
G11B 7/245 20130101;
G03H 2001/0264 20130101; C08K 5/0008 20130101; C08G 18/792
20130101; C07D 273/04 20130101; C08G 18/4277 20130101; C08G 18/7887
20130101; C08G 18/022 20130101 |
Class at
Publication: |
430/2 |
International
Class: |
G03C 1/73 20060101
G03C001/73 |
Claims
1. A polyurethane composition comprising A) one or more
iminooxadiazinedione-group-containing polyisocyanates, B) one or
more polyfunctional, isocyanate-reactive compounds, C) one or more
compounds having groups which react on exposure to actinic
radiation with ethylenically unsaturated compounds with
polymerization (radiation-curing groups), D) optionally one or more
free radical stabilizers and E) one or more photoinitiators.
2. A polyurethane composition according to claim 1, wherein at
least 60% by weight of the polyisocyanates of component A) are
based on aliphatic and/or cycloaliphatic di- and/or
triisocyanates.
3. A polyurethane composition according to claim 1, wherein one or
more compounds of the group consisting of 9-vinylcarbazole,
vinylnaphthalene, bisphenol A diacrylate, tetrabromobisphenol A
diacrylate, 1,4-bis(2-thionaphthyl)-2-butyl acrylate,
pentabromophenyl acrylate, naphthyl acrylate and
propane-2,2-diylbis[(2,6-dibromo-4,1-phenylene)oxy(2-{[3,3,3-tris(4-chlor-
ophenyl)propanoyl]oxy}propane-3,1-diyl)oxyethane-2,1-diyl]diacrylate
are used in C).
4. A polyurethane composition according to claim 1, wherein the
molar ratio of NCO to OH groups therein is from 0.90 to 1.25.
5. A polymeric plastic prepared from the polyurethane composition
according to claim 1.
6. A polymeric plastic according to claim 5, wherein the polymeric
plastic is a layer or molding.
7. A polymeric plastic according to claim 5, wherein the polymeric
plastic has a glass transition temperature of less than -40.degree.
C.
8. Holographic media comprising a polyurethane composition
according to claim 1.
9. Holographic media comprising at least one polymeric plastic
according to claim 5.
Description
CROSS-REFERENCE TO RELATED APPLICATION
[0001] This application claims priority under 35 U.S.C. .sctn.
119(e) to provisional application Ser. No. 60/922,989, filed Apr.
11, 2007 the disclosure of which is incorporated by reference for
all useful purposes
FIELD OF THE INVENTION
[0002] The present invention relates to polyurethane systems which
cure by radiation and thermal action with crosslinking, and the use
thereof for the production of holographic media.
BACKGROUND OF THE INVENTION
[0003] In the production of holographic media, as described in U.S.
Pat. No. 6,743,552, information is stored in a polymer layer which
substantially consists of a matrix polymer and very special
polymerizable monomers distributed uniformly therein. This matrix
polymer may be based on polyurethane. It is prepared as a rule
starting from NCO-functional prepolymers which are crosslinked with
polyols, such as polyethers or polyesters, with urethane
formation.
[0004] However, what is problematic is that low viscosities of the
reaction mixtures are required for an efficient production of such
holographic media but, on the other hand, solvents for setting
viscosity are undesired. A further problem is that the curing under
urethanization often lasts too long.
[0005] Systems comprising polyisocyanates, polyols and
radiation-curing compounds, such as photochemically crosslinking
reactive diluents, are known in individual cases from the area of
coating technology (U.S. Pat. No. 4,247,578, DE 197 09 560). Polyol
components mentioned are substantially polyether- or
polyester-based ones or polyacrylatepolyols. However, indications
as to how a rapid curing can be achieved at low viscosity are not
given.
SUMMARY OF THE INVENTION
[0006] It was an object of the present invention to provide
polyurethane systems which are suitable for the production of
storage layers for holographic storage media and which, in the
solvent-free state, have relatively low viscosities and in addition
a rapid curing.
[0007] It has now been found that excellent compatibility of matrix
polymer with the unsaturated monomers is obtained precisely when
iminooxadiazinedione-group-containing polyisocyanates are used as a
building block for the matrix polymers.
[0008] The invention relates to polyurethane systems comprising
[0009] A) iminooxadiazinedione-group-containing polyisocyanates,
[0010] B) polyfunctional, isocyanate-reactive compounds, [0011] C)
compounds having groups which react on exposure to actinic
radiation with ethylenically unsaturated compounds with
polymerization (radiation-curing groups), [0012] D) optionally free
radical stabilizers and [0013] E) photoinitiators.
DETAILED DESCRIPTION OF THE INVENTION
[0014] As used herein in the specification and claims, including as
used in the examples and unless otherwise expressly specified, all
numbers may be read as if prefaced by the word "about", even if the
term does not expressly appear. Also, any numerical range recited
herein is intended to include all sub-ranges subsumed therein.
[0015] Polyisocyanates of component A which may be used are per se
all NCO-functional compounds having at least one
iminooxadiazinedione group.
[0016] These may have an aromatic, araliphatic, aliphatic or
cycloaliphatic basis. Iminooxadiazinedione-group-free mono-, di-,
tri- or polyisocyanates can also be used in addition.
[0017] The basis for such isocyanates are, for example, butylene
diisocyanate, hexamethylene diisocyanate (HDI), isophorone
diisocyanate (IPDI), 1,8-diisocyanato-4-(isocyanatomethyl)octane,
2,2,4- and/or 2,4,4-trimethylhexamethylene diisocyanate, the
isomeric bis(4,4'-isocyanatocyclohexyl)methanes and mixtures
thereof having any desired isomer content,
isocyanatomethyl-1,8-octane diisocyanate, 1,4-cyclohexylene
diisocyanate, the isomeric cyclohexanedimethylene diisocyanates,
1,4-phenylene diisocyanate, 2,4- and/or 2,6-toluene diisocyanate,
1,5-naphthylene diisocyanate, 2,4'- or 4,4'-diphenylmethane
diisocyanate and/or triphenylmethane 4,4',4''-triisocyanate are
suitable.
[0018] The use of derivatives of monomeric di- or triisocyanates
having urethane, urea, carbodiimides, acylurea, isocyanurate,
allophanate, biuret, oxadiazinetrione, uretdione and/or
iminooxadiazinedione structures is also possible.
[0019] The use of polyisocyanates based on aliphatic and/or
cycloaliphatic di- or triisocyanates of the abovementioned type is
preferred.
[0020] The proportion of iminooxadiazinedione-group-free
isocyanates, based on the total amount of component A), is
preferably not more than 90% by weight, particularly preferably not
more than 50% by weight and very particularly preferably not more
than 40% by weight.
[0021] Iminooxadiazinedione-group-containing polyisocyanates based
on hexamethylene diisocyanate are particularly preferred.
[0022] The proportion of iminooxadiazinedione groups, based on the
total amount of trimer structures in the polyisocyanates of the
present invention, is preferably more than 30 mol %, particularly
preferably more than 35 mol %, very particularly preferably more
than 40 mol %.
[0023] Such polyisocyanates having relatively high
iminooxadiazinedione proportions are, according to EP-A 0 798 299,
obtainable by trimerization of corresponding isocyanate monomers or
mixtures of different monomers in the presence of special
catalysts. Particularly suitable catalysts are hydrogen
(poly)fluorides of the composition {M[nF.sup.-*(HF).sub.m]}, in
which m/n>0 and M is a cation having a charge of n or a n-valent
organic radical.
[0024] The NCO groups of the compounds of component A) may also be
completely or partly blocked with blocking agents customary known
per se to the person skilled in the art.
[0025] Examples of these are alcohols, lactams, oximes, malonic
esters, alkyl acetoacetates, triazoles, phenols, imidazoles,
pyrazoles and amines, such as, for example, butanone oxime,
diisopropylamine, 1,2,4-triazole, dimethyl-1,2,4-triazole,
imidazole, diethyl malonate, ethyl acetoacetate, acetone oxime,
3,5-dimethylpyrazole, .epsilon.-caprolactam,
N-tert-butylbenzylamine, cyclopentanone carboxyethyl ester or any
desired mixtures of these blocking agents.
[0026] All polyfunctional, isocyanate-reactive compounds which have
on average at least 1.5 isocyanate-reactive groups per molecule can
be used in component B). Isocyanate-reactive groups in the context
of the present invention are preferably hydroxyl, amino or thio
groups.
[0027] Suitable polyfunctional, isocyanate-reactive compounds are,
for example, polyester, polyether, polycarbonate,
poly(meth)acrylate and/or polyurethane polyols.
[0028] Suitable polyester polyols are, for example, linear
polyester diols or branched polyester polyols, as obtained in known
manner from aliphatic, cycloaliphatic or aromatic di- or
polycarboxylic acids or their anhydrides with polyhydric alcohols
having an OH functionality of .gtoreq.2.
[0029] Examples of such di- or polycarboxylic acids or anhydrides
are succinic, glutaric, adipic, pimelic, suberic, azelaic, sebacic,
nonanedicarboxylic, decanedicarboxylic, terephthalic, isophthalic,
o-phthalic, tetrahydrophthalic, hexahydrophthalic or trimellitic
acid and acid anhydrides, such as o-phthalic, trimellitic or
succinic anhydride, or any desired mixtures thereof with one
another.
[0030] Examples of such suitable alcohols are ethanediol, di-, tri-
or tetraethylene glycol, 1,2-propanediol, di-, tri- or
tetrapropylene glycol, 1,3-propanediol, 1,4-butanediol,
1,3-butanediol, 2,3-butanediol, 1,5-pentanediol, 1,6-hexanediol,
2,2-dimethyl-1,3-propanediol, 1,4-dihydroxycyclohexane,
1,4-dimethylolcyclohexane, 1,8-octanediol, 1,10-decanediol,
1,12-dodecandiol, trimethylolpropane, glycerol or any desired
mixtures thereof with one another.
[0031] The polyester polyols may also be based on natural raw
materials, such as caster oil. It is also possible for the
polyester polyols to be based on homo- or copolymers of lactones,
as can preferably be obtained by an addition reaction of lactones
or lactone mixtures, such as butyrolactone, .epsilon.-caprolactone
and/or methyl-.epsilon.-caprolactone, with hydroxyl-functional
compounds, such as polyhydric alcohols having an OH functionality
of .gtoreq.2, for example of the abovementioned type.
[0032] Such polyester polyols preferably have number average molar
masses of from 400 to 4000 g/mol, particularly preferably from 500
to 2000 g/mol. Their OH functionality is preferably from 1.5 to
3.5, particularly preferably from 1.8 to 3.0.
[0033] Suitable polycarbonate polyols are accessible in a manner
known per se by reacting organic carbonates or phosgene with diols
or diol mixtures.
[0034] Suitable organic carbonates are dimethyl, diethyl and
diphenyl carbonate.
[0035] Suitable diols or diol mixtures comprise the polyhydric
alcohols mentioned per se in relation to the polyester segments and
having an OH functionality of .gtoreq.2, preferably 1,4-butanediol,
1,6-hexanediol and/or 3-methylpentanediol.
[0036] Such polycarbonate polyols preferably have number average
molar masses of from 400 to 4000 g/mol, particularly preferably
from 500 to 2000 g/mol. The OH functionality of these polyols is
preferably from 1.8 to 3.2, particularly preferably from 1.9 to
3.0.
[0037] Suitable polyether polyols are polyadducts of cyclic ethers
with OH- or NH-functional initiator molecules, which polyadducts
optionally have a block structure.
[0038] Suitable cyclic ethers are, for example, styrene oxides,
ethylene oxide, propylene oxide, tetrahydrofuran, butylene oxide,
epichlorohydrin and any desired mixtures thereof.
[0039] Initiators which may be used are the polyhydric alcohols
mentioned per se in relation to the polyester segments and having
an OH functionality of .gtoreq.2 and primary or secondary amines
and aminoalcohols.
[0040] Such polyether polyols preferably have number average molar
masses of from 250 to 10 000 g/mol, particularly preferably from
500 to 4000 g/mol and very particularly preferably from 600 to 2000
g/mol. The OH functionality is preferably from 1.5 to 4.0,
particularly preferably from 1.8 to 3.0.
[0041] In addition, aliphatic, araliphatic or cycloaliphatic di-,
tri- or polyfunctional alcohols which have a low molecular weight,
i.e. molecular weights of less than 500 g/mol, and are short-chain,
i.e. contain 2 to 20 carbon atoms, are also suitable as
polyfunctional, isocyanate-reactive compounds as constituents of
component B).
[0042] These may be, for example, ethylene glycol, diethylene
glycol, triethylene glycol, tetraethylene glycol, dipropylene
glycol, tripropylene glycol, 1,2-propanediol, 1,3-propanediol,
1,4-butanediol, neopentyl glycol, 2-ethyl-2-butylpropanediol,
trimethylpentanediol, diethyloctanediol positional isomers,
1,3-butylene glycol, cyclohexanediol, 1,4-cyclohexanedimethanol,
1,6-hexanediol, 1,2- and 1,4-cyclohexanediol, hydrogenated
bisphenol A (2,2-bis(4-hydroxycyclohexyl)propane),
2,2-dimethyl-3-hydroxypropyl 2,2-dimethyl-3-hydroxypropionate.
Examples of suitable triols are trimethylolethane,
trimethylolpropane or glycerol. Suitable alcohols having a higher
functionality are ditrimethylolpropane, pentaerythritol,
dipentaerythritol or sorbitol.
[0043] Also suitable are aminoalcohols, such as, for example,
ethanolamine, diethanolamine, 2-(N,N-dimethylamino)ethylamine,
N-methyldiethanolamine, N-methyldiisopropanolamine,
N-ethyldiethanolamine, N-ethyldiisopropanolamine,
N,N'-bis(2-hydroxyethyl)perhydropyrazine,
N-methylbis(3-aminopropyl)amine, N-methylbis(2-aminoethyl)amine,
N,N'-,N''-trimethyldiethylenetriamine, N,N-dimethylaminoethanol,
N,N-diethylaminoethanol, 1-N,N-diethylamino-2-aminoethane,
1-N,N-diethylamino-3-aminopropane,
2-dimethylaminomethyl-2-methyl-1,3-propanediol,
N-isopropyldiethanolamine, N-butyldiethanolamine,
N-isobutyldiethanolamine, N-oleyldiethanolamine,
N-stearyldiethanolamine, oxyethylated coconut fatty amine,
N-allyldiethanolamine, N-methyldiisopropanolamine,
N,N-propyldiisopropanolamine, N-butyldiisopropanolamine and/or
N-cyclohexyldiisopropanolamine.
[0044] In component C), .alpha.,.beta.-unsaturated carboxylic acid
derivatives, such as acrylates, methacrylates, maleates, fumarates,
maleimides, acrylamides and furthermore vinyl ethers, propylene
ether, allyl ether and compounds containing dicyclopentadienyl
units and olefinically unsaturated compounds, such as styrene,
.alpha.-methylstyrene, vinyltoluene, vinylcarbazole, olefins, such
as, for example, 1-octene and/or 1-decene, vinyl esters, such as,
for example, .RTM.VeoVa 9 and/or .RTM.VeoVa 10 from Shell,
(meth)acrylonitrile, (meth)acrylamide, methacrylic acid, acrylic
acid and any desired mixtures thereof may be used. Acrylates and
methacrylates are preferred, and acrylates are particularly
preferred.
[0045] Esters of acrylic acid or methacrylic acid are generally
referred to as acrylates or methacrylates. Examples of acrylates
and methacrylates which may be used are methyl acrylate, methyl
methacrylate, ethyl acrylate, ethyl methacrylate, ethoxyethyl
acrylate, ethoxyethyl methacrylate, n-butyl acrylate, n-butyl
methacrylate, tert-butyl acrylate, tert-butyl methacrylate, hexyl
acrylate, hexyl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl
methacrylate, butoxyethyl acrylate, butoxyethyl methacrylate,
lauryl acrylate, lauryl methacrylate, isobornyl acrylate, isobornyl
methacrylate, phenyl acrylate, phenyl methacrylate, p-chlorophenyl
acrylate, p-chlorophenyl methacrylate, p-bromophenyl acrylate,
p-bromophenyl methacrylate, trichlorophenyl acrylate,
trichlorophenyl methacrylate, tribromophenyl acrylate,
tribromophenyl methacrylate, pentachlorophenyl acrylate,
pentachlorophenyl methacrylate, pentabromophenyl acrylate,
pentabromophenyl methacrylate, pentabromobenzyl acrylate,
pentabromobenzyl methacrylate, phenoxyethyl acrylate, phenoxyethyl
methacrylate, phenoxyethoxyethyl acrylate, phenoxyethoxyethyl
methacrylate, 2-naphthyl acrylate, 2-naphthyl methacrylate,
1,4-bis-(2-thionaphthyl)-2-butyl acrylate,
1,4-bis-(2-thionaphthyl)-2-butyl methacrylate, bisphenol A
diacrylate, bisphenol A dimethacrylate, tetrabromobisphenol A
diacrylate, tetrabromobisphenol A dimethacrylate,
2,2,2-trifluoroethyl acrylate, 2,2,2-trifluoroethyl methacrylate,
1,1,1,3,3,3-hexafluoroisopropyl acrylate,
1,1,1,3,3,3-hexafluoroisopropyl methacrylate,
2,2,3,3,3-pentafluoropropyl acrylate and/or
2,2,3,3,3-pentafluoropropyl methacrylate.
[0046] Epoxy acrylates also suitable as component C) can be
obtained as reaction products of bisphenol A diglycidyl ether with
hydroxyalkyl(meth)acrylates and carboxylic acids, the bisphenol A
diglycidyl ether first being reacted with
hydroxyalkyl(meth)acrylate with catalysis by Lewis acid and this
hydroxyl-functional reaction product then being esterified with a
carboxylic acid by a method known to the person skilled in the art.
Bisphenol A diglycidyl ether itself and brominated variants, such
as, for example, tetrabromobisphenol A diglycidyl ether (from Dow
Chemical, D.E.R. 542), can advantageously be used as the diepoxide.
All hydroxyl-functional acrylates described above can be used as
hydroxyalkyl(meth)acrylates, in particular 2-hydroxyethyl acrylate,
hydroxypropyl acrylate, 4-hydroxybutyl acrylate,
poly(.epsilon.-caprolactone) mono (meth)acrylates and poly(ethylene
glycol) mono(meth)acrylates. All monofunctional carboxylic acids
are in principle suitable as the carboxylic acid, in particular
those having aromatic substituents.
Propane-2,2-diylbis[(2,6-dibromo-4,1-phenylene)oxy(2-{[3,3,3-tris(4-chlor-
ophenyl)propanoyl]oxy}propane-3,1-diyl)oxyethane-2,1-diyl]diacrylate
has proved to be a preferred compound of this class of epoxy
acrylates.
[0047] Vinylaromatics suitable for component C) are styrene,
halogenated derivatives of styrene, such as, for example,
2-chlorostyrene, 3-chlorostyrene, 4-chlorostyrene, 2-bromostyrene,
3-bromostyrene, 4-bromostyrene, p-(chloromethyl)styrene,
p-(bromomethyl)styrene or 1-vinylnaphthalene, 2-vinylnaphthalene,
2-vinylanthracene, N-vinylpyrrolidone, 9-vinylanthracene,
9-vinylcarbazole or difunctional compounds, such as divinylbenzene.
Vinyl ethers, such as, for example, butyl vinyl ether, are also
suitable.
[0048] Preferred compounds of component C) are 9-vinylcarbazole,
vinylnaphthalene, bisphenol A diacrylate, tetrabromobisphenol A
diacrylate, 1,4-bis-(2-thionaphthyl)-2-butyl acrylate,
pentabromophenyl acrylate, naphthyl acrylate and
propane-2,2-diylbis[(2,6-dibromo-4,1-phenylene)oxy(2-{[3,3,3-tris(4-chlor-
ophenyl)propanoyl]-oxy}propane-3,1-diyl)oxyethane-2,1-diyl]diacrylate.
[0049] One or more free radical stabilizers are used as component
D). Inhibitors and antioxidants, as described in "Methoden der
organischen Chemie [Methods of Organic Chemistry]" (Houben-Weyl),
4th edition, volume XIV/1, page 433 et seq., Georg Thieme Verlag,
Stuttgart 1961, are suitable. Suitable classes of substances are,
for example, phenols, such as for example,
2,6-di-tert-butyl-4-methylphenol, cresols, hydroquinones, benzyl
alcohols, such as benzhydrol, optionally also quinones, such as,
for example, 2,5-di-tert-butylquinone, optionally also aromatic
amines, such as diisopropylamine or phenothiazine. Preferred free
radical stabilizers are 2,6-di-tert-butyl-4-methylphenol,
phenothiazine and benzhydrol.
[0050] One or more photoinitiators are used as component E). These
are usually initiators which can be activated by actinic radiation
and initiate a free radical polymerization of the corresponding
polymerizable groups. Photoinitiators are commercially sold
compounds known per se, a distinction being made between
monomolecular (type I) and bimolecular (type II) initiators. (Type
I) systems are, for example, aromatic ketone compounds, e.g.
benzophenones, in combination with tertiary amines,
alkylbenzophenones, 4,4'-bis(dimethylamino)benzophenone (Michler's
ketone), anthrone and halogenated benzophenones or mixtures of said
types. (Type II) initiators, such as benzoin and its derivatives,
benzyl ketals, acylphosphine oxides, e.g.
2,4,6-trimethylbenzoyldiphenylphosphine oxide, bisacylophosphine
oxides, phenylglyoxylic acid esters, camphorquinone,
.alpha.-aminoalkylphenones, .alpha.,.alpha.-dialkoxyacetophenones,
1-[4-(phenylthio)phenyl]octane-1,2-dione-2-(O-benzoyloxime) and
.alpha.-hydroxyalkylphenones, are furthermore suitable. The
photoinitiator systems described in EP-A 0223587 and consisting of
a mixture of an ammonium arylborate and one or more dyes can also
be used as a photoinitiator. For example, tetrabutylammonium
triphenylhexylborate, tetrabutylammonium
tris-(3-fluorophenyl)hexylborate and tetramethylammonium
tris-(3-chloro-4-methylphenyl)hexylborate are suitable as the
ammonium arylborate. Suitable dyes are, for example, new methylene
blue, thionine, Basic Yellow, pinacyanol chloride, rhodamine 60,
gallocyanine, ethyl violet, Victoria Blue R, Celestine Blue,
quinaldine red, crystal violet, brilliant green, Astrazon Orange G,
Darrow Red, pyronine Y, Basic Red 29, pyrillium 1, cyanine,
methylene blue and azure A.
[0051] It may also be advantageous to use mixture of these
compounds. Depending on the radiation source used for curing, type
and concentration must be adapted to photoinitiator in a manner
known to the person skilled in the art. Further details are
described, for example, in P. K. T. Oldring (Ed.), Chemistry &
Technology of UV & EB Formulations For Coatings, Inks &
Paints, vol. 3, 1991, SITA Technology, London, pages 61-328.
[0052] Preferred photoinitiators are
2,4,6-trimethylbenzoyldiphenylphosphine oxide,
1-[4-(phenylthio)phenyl]octane-1,2-dione-2-(O-benzoyloxime) and
mixtures of tetrabutylammonium tris(3-fluorophenyl)hexylborate,
tetramethylammonium tris(3-chloro-4-methylphenyl)hexylborate with
dyes, such as, for example, methylene blue, new methylene blue,
azure A, pyrillium 1, cyanine, gallocyanine, brilliant green,
crystal violet and thionine.
[0053] Furthermore, one or more catalysts may be used in the PU
systems according to the invention. These preferably catalyze the
urethane formation. Amines and metal compounds of the metals tin,
zinc, iron, bismuth, molybdenum, cobalt, calcium, magnesium and
zirconium are preferably suitable for this purpose. Tin octanoate,
zinc octanoate, dibutyltin dilaurate, dimethyltin dicarboxylate,
iron(III) acetylacetonate, iron(II) chloride, zinc chloride,
tetraalkylammonium hydroxides, alkali metal hydroxides, alkali
metal alcoholates, alkali metal salts of long-chain fatty acids
having 10 to 20 carbon atoms and optionally OH side groups, lead
octanoate or tertiary amines, such as triethylamine, tributylamine,
dimethylbenzylamine, dicyclohexylmethylamine,
dimethylcyclohexylamine, N,N,N',N'-tetramethyldiaminodiethylether,
bis(dimethylaminopropyl)urea, N-methyl- or N-ethylmorpholine,
N,N'-dimorpholinodiethyl ether (DMDEE), N-cyclohexylmorpholine,
N,N,N',N'-tetramethylethylenediamine,
N,N,N',N'-tetramethylbutanediamine,
N,N,N',N'-tetramethyl-1,6-hexanediamine,
pentamethyldiethylenetriamine, dimethylpiperazine,
N-dimethylaminoethylpiperidine, 1,2-dimethylimidazole,
N-hydroxypropylimidazole, 1-azabicyclo[2.2.0]octane,
1,4-diazabicyclo[2.2.2]octane (Dabco), or alkanolamine compounds
such as triethanolamine, triisopropanolamine, N-methyl- and
N-ethyldiethanolamine, dimethylaminoethanol,
2-(N,N-dimethylaminoethoxy)ethanol, or
N-tris(dialkylaminoalkyl)hexahydrotriazines, e.g.
N,N',N-tris(dimethylaminopropyl)-s-hexahydrotriazine,
diazabicyclononane, diazabicycloundecane,
1,1,3,3-tetramethylguanidine,
1,3,4,6,7,8-hexahydro-1-methyl-2H-pyrimido(1,2-a)pyrimidine, are
particularly preferred.
[0054] Particularly preferred catalysts are dibutyltin dilaurate,
dimethyltin dicarboxylate, iron(III) acetylacetonate,
1,4-diazabicyclo[2.2.2]octane, diazabicyclononane,
diazabicycloundecane, 1,1,3,3-tetramethylguanidine and
1,3,4,6,7,8-hexahydro-1-methyl-2H-pyrimido(1,2-a)pyrimidine.
[0055] In addition, further auxiliaries and additives may also be
present in the PU systems according to the invention. These are,
for example, solvents, plasticizers, leveling agents, antifoams or
adhesion promoters, but also polyurethanes, thermoplastic polymers,
oligomers, and further compounds having functional groups, such as,
for example acetals, epoxide, oxetanes, oxazolines, dioxolanes
and/or hydrophilic groups, such as, for example, salts and/or
polyethylene oxides.
[0056] Preferably used solvents are readily volatile solvents
having good compatibility with the 2-component formulations
according to the invention, for example ethyl acetate, butyl
acetate or acetone.
[0057] Liquids having good dissolution properties, low volatility
and a high boiling point are preferably used as plasticizers; these
may be, for example, diisobutyl adipate, di-n-butyl adipate,
dibutyl phthalate, non-hydroxy-functional polyethers, such as, for
example, polyethylene glycol dimethyl ether having a number average
molar mass of from 250 g/mol to 2000 g/mol or polypropylene glycol
and mixtures of said compounds.
[0058] It may also be advantageous simultaneously to use a
plurality of additives of one type. Of course, it may also be
advantageous to use a plurality of additives of a plurality of
types.
[0059] The mixture of the components B) to E) and optionally
catalysts and auxiliaries and additives usually consists of
24.999-99.899% by weight of component B) 0.1-75% by weight of
component C) 0-3% by weight of component D) 0.001-5% by weight of
component E) 0-4% by weight of catalysts 0-50% by weight of
auxiliaries and additives.
[0060] The mixture preferably consists of
86.998-97.998% by weight of component B) 2-13% by weight of
component C) 0.001-1% by weight of component D) 0.001-1% by weight
of component E) 0-2% by weight of catalysts 0-15% by weight of
auxiliaries and additives.
[0061] The mixture likewise preferably consists of
44.8-87.8% by weight of component B) 12.5-55% by weight of
component C) 0.1-3% by weight of component D) 0.1-3% by weight of
component E) 0-3% by weight of catalysts 0-50% by weight of
auxiliaries and additives.
[0062] The molar ratio of NCO to OH is typically from 0.5 to 2.0,
preferably from 0.90 to 1.25.
[0063] The PU systems according to the invention are usually
obtained by a procedure in which first all components, except for
the polyisocyanates A) are mixed with one another. This can be
achieved by all methods and apparatuses known per se to the person
skilled in the art from mixing technology, such as, for example
stirred vessels or both dynamic and static mixers. The temperatures
during this procedure are from 0 to 100.degree. C., preferably from
10 to 80.degree. C., particularly preferably from 20 to 60.degree.
C. This mixture can immediately be further processed or can be
stored as a storage-stable, intermediate, optionally for several
months.
[0064] If necessary, degassing can also be carried out under a
vacuum of, for example, 1 mbar.
[0065] The mixing with the polyisocyanate component A) is then
effected shortly before the application, it likewise being possible
to use the customary mixing techniques. However, apparatuses
without any, or with only little dead space are preferred.
Furthermore, methods in which the mixing is effected within a very
short time and with very vigorous mixing of the two mixed
components are preferred. Dynamic mixers, in particular those in
which the components A) and B) to E) first come into contact with
one another in the mixer are particularly suitable for this
purpose. This mixing can be effected at temperatures of from 0 to
80.degree. C., preferably at from 5 to 50.degree. C., particularly
preferably from 10 to 40.degree. C. The mixture of the two
components A and B can optionally also be degassed after the mixing
under a vacuum of, for example, 1 mbar in order to remove the
residual gases and to prevent the formation of bubbles in the
polymer layer. The mixing gives a clear, liquid formulation which,
depending on the composition, cures within a few seconds to a few
hours at room temperature.
[0066] The PU systems according to the invention are preferably
adjusted so that the curing at room temperature begins within
minutes to one hour. In a preferred embodiment, the curing is
accelerated by heating the formulation after mixing to temperatures
between 30 and 180.degree. C., preferably from 40 to 120.degree.
C., particularly preferably from 50 to 100.degree. C.
[0067] Immediately after mixing of all components, the polyurethane
systems according to the invention have viscosities at room
temperature of, typically from 10 to 100 000 mPas, preferably from
100 to 20 000 mPas, particularly preferably from 200 to 10 000
mPas, especially preferably from 500 to 1500 mPas, so that they
have very good processing properties even in solvent-free form. In
a solution with suitable solvents viscosities at room temperature
of less than 10 000 mPas, preferably less than 2000 mPas,
particularly preferably less than 500 mPas, can be established.
[0068] Systems which cure in an amount of 15 g and with a catalyst
content of 0.004% within 4 hours or at a catalyst content of 0.02%
in less than 10 minutes have proven to be advantageous.
[0069] The present invention furthermore relates to the polymers
obtainable from PU systems according to the invention.
[0070] These preferably have glass transition temperatures of less
than -10.degree. C., preferably less than -25.degree. C. and
particularly preferably less than 40.degree. C.
[0071] According to a preferred process the formulation according
to the invention is applied directly after mixing to a substrate it
being possible to use all customary methods known to the person
skilled in the art in coating technology; in particular, the
coating can be applied by knife coating, casting, printing, screen
printing, spraying or inkjet printing.
[0072] The substrates may be plastic, metal, wood, paper, glass,
ceramic and composite materials comprising a plurality of these
materials, in a preferred embodiment the substrate having the form
of a sheet.
[0073] In a preferred embodiment, the coating of the substrate with
the formulation is carried out in a continuous process. As a rule
the formulation according to the invention is applied as a film
having a thickness of from 5 mm to 1 .mu.m, preferably from 500
.mu.m to 5 .mu.m, particularly preferably from 50 .mu.m to 8 .mu.m
and very particularly preferably from 25 .mu.l to 10 .mu.m to the
substrate.
[0074] In the case of a sheet as a substrate, flexible, coated
sheets are thus obtained, which sheets, in the case of a continuous
process, can be rolled up after curing and thus stored over several
months.
[0075] In a further preferred embodiment, the formulation is
applied so that it is covered on both sides by transparent
substrates, in particular plastic or glass, for this purpose the
formulation being poured between the substrates held at an exact
spacing of from 1 to 2 mm, preferably from 1.2 to 1.8 mm,
particularly preferably from 1.4 to 1.6 mm, in particular 1.5 mm,
and the substrates being kept at the exact spacing until the
formulation has completely solidified and can no longer flow.
[0076] The materials used as the substrate can of course have a
plurality of layers. It is possible both for the substrate to
consist of layers of a plurality of different materials and for it
additionally to have, for example, coatings having additional
properties, such as improved adhesion, enhanced hydrophobic or
hydrophilic properties, improved scratch resistance, antireflection
properties in certain wavelength ranges, improved evenness of the
surface, etc.
[0077] The materials obtained by one of the methods described can
then be used for the recording of holograms. For this purpose, two
light beams are caused to interfere in the material by a method
known to the person skilled in the art of holography (P. Hariharan,
Optical Holography 2nd Edition, Cambridge University Press, 1996)
so that a hologram forms. The exposure of the hologram can be
effected both by continuous and by pulsed irradiation. It is
optionally also possible to produce more than one hologram by
exposure in the same material and at the same point, it being
possible to use, for example, the angle multiplexing method known
to the person skilled in the art of holography. After the exposure
of the hologram, the material can optionally also be exposed to a
strong, broadband light source and the hologram then used without
further necessary processing steps. The hologram can optionally
also be further processed by further processing steps, for example
transfer to another substrate, deformed, insert-molded, adhesively
bonded to another surface, or covered with a scratch-resistant
coating.
[0078] The holograms produced by one of the processes described can
serve for data storage, for the representation of images which
serve, for example, for the three-dimensional representation of
persons or objects and for the authentification of a person or of
an article, for the production of an optical element having the
function of a lens, a mirror, a filter, a diffusion screen, a
diffraction element, an optical waveguide and/or a mask.
[0079] The invention therefore furthermore relates to the use of
the PU systems according to the invention in the production of
holographic media, and to the holographic media as such.
EXAMPLES
[0080] The viscosities of the respective formulations were measured
without the urethanization catalyst (component B5). All viscosities
were determined using a cone-and-plate viscometer (Anton Paar MCR
51 brand, viscosity over increasing shear rate 10-1000/sec) at
23.RTM.C.
[0081] The curing time was determined in each case by the following
method:
[0082] 15 grams of the respective formulation without the
urethanization catalyst (component B5) were weighed into a
polyethylene plastic vessel and completely mixed by means of a
suitable mixer. Thereafter, the urethanization catalyst (component
B5) was added and likewise completely mixed in. Thereafter, a metal
bow was inserted into the mixture and was pulled out of the mixture
and inserted again at regular intervals until it was no longer
possible to pull the metal bow out of the then cured mixture. The
curing time was taken as the period between the catalyst addition
and the discovery that the metal bow could no longer be pulled out
of the material.
TABLE-US-00001 Two-component formulations A to G Formulation A B C
D E F G Component A 4.995 g of 4.856 g of 5.024 g of 4.856 g of
7.292 g of 4.790 g of 4.829 g of Desmodur Desmodur Desmodur
Desmodur Desmodur Desmodur XP Desmodur VP N100* N3200* N3300*
N3600* N3800* 2410* LS 2294* Component B1 8.504 g 8.643 g 8.475 g
8.643 g 6.207 g 8.710 g 8.670 g Component B2 (6%) 0.900 g 0.900 g
0.900 g 0.900 g 0.900 g 0.900 g 0.900 g Component B3 (0.5%) 0.075 g
0.075 g 0.075 g 0.075 g 0.075 g 0.075 g 0.075 g Component B4 (0.5%)
0.075 g 0.075 g 0.075 g 0.075 g 0.075 g 0.075 g 0.075 g Component
B5 (0.004%) 0.006 g 0.006 g 0.006 g 0.006 g 0.006 g 0.006 g 0.006 g
Component B6 (3%) 0.45 g 0.45 g 0.45 g 0.45 g 0.45 g 0.45 g 0.45 g
Viscosity in mPa s at 1280 910 981 725 2160 707 728 23.degree. C.**
Curing time in min at 436 470 280 298 200 232 227 23.degree. C.
ambient temperature *Desmodur N100: HDI biuret polyisocyanate (NCO
content: 22.0%; commercial product of Bayer MaterialScience AG);
Desmodur N3200: HDI biuretpolyisocyanate (NCO content: 23.0%;
commercial product of Bayer MaterialScience AG); Desmodur N3300:
HDI isocyanurate polyisocyanate (NCO content: 21.8%; commercial
product of Bayer MaterialScience AG); Desmodur N3800: elastified
HDI trimer prepolymer (NCO content: 11.0%; commercial product of
Bayer MaterialScience AG); Desmodur N3600: HDI isocyanurate
polyisocyanate (NCO content: 23.0%; commercial product of Bayer
MaterialScience AG); Desmodur XP2410: HDI iminooxadiazinedione
polyisocyanate (NCO content: 23.5%; experimental product of Bayer
Material Science AG); Desmodur VP LS 2294: HDI iminooxadiazinedione
polyisocyanate (NCO content 23.2%; experimental product of Bayer
MaterialScience AG). Component B1: Poly(caprolactone)polyol; Mn
about 650 g/mol, equivalent weight about 325 g/mol OH Component B2:
Propane-2,2-diylbis[(2,6-dibromo-4,1-phenylene)oxy(2-{[3,3,3-tris(4-chlor-
opheny)propanoyl]oxy}propane-3,1-diyl)oxyethane-2,1-diyl]
diacrylate Component B3: 2,4,6-Trimethylbenzoyldiphenylphosphine
oxide (Darocure TPO, commercial product of Ciba Speciality
Chemicals) Component B4: Benzhydrol Component B5: Dibutyltin
dilaurate Component B6: Dibutyl phthalate **Viscosities were
measured in the absence of component B5.
[0083] The values stated in the table show that the formulations G
and H according to the invention have the overall most advantageous
property combination comprising low viscosity and short curing
time.
[0084] All the references described above are incorporated by
reference in its entirety for all useful purposes.
[0085] While there is shown and described certain specific
structures embodying the invention, it will be manifest to those
skilled in the art that various modifications and rearrangements of
the parts may be made without departing from the spirit and scope
of the underlying inventive concept and that the same is not
limited to the particular forms herein shown and described.
* * * * *